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Invasive Group A Streptococcal Infection

French Pediatric Nationwide Observatory of Invasive Group A Streptococcal Infection (in Childen for 0 to 18 Ages)

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT05788861
Acronym
ISAI
Enrollment
100
Registered
2023-03-29
Start date
2022-09-01
Completion date
2026-09-01
Last updated
2024-02-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Medical Care, Medical Complications, Outcome, Fatal, Risk Factors, Sepsis Due to Streptococcus, Group A, Severe Infection, Strain, Therapy, Virulence Factors

Brief summary

This study is observational, retrospective and prospective study in pediatric patients hospitalized with invasive streptococcal A infection

Detailed description

The main of this study is to identify and record cases of invasive and severe infections due to Streptococcus pyogenes. In order to evaluate the incidence of severe forms of disease and the possible contributing factors, and to optimize their management. Admitted patients to intensive care or critical care units in reported via Santé Publique France may also be included in this study. Secondly, epidemiological, clinical, bacteriological data of all severe or not cases, of group A Streptococcal infections will be compiled to describe their characteristics, and try to explain this recrudescence as well as possible.

Interventions

None listed

Sponsors

Association Clinique Thérapeutique Infantile du val de Marne
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
1 Days to 17 Years
Healthy volunteers
No

Inclusion criteria

* Age\<18 years * Documented invasive Group A Streptococcus infection (identification of GAS in a normally sterile site or from another site in case of toxin shock or necrotizing dermo-hypodermatitis)

Exclusion criteria

* Opposition of the patient or his/her legal representative

Design outcomes

Primary

MeasureTime frameDescription
Hospitalisation1 yearHow long patient was hospitalised during this infection
Treatments provided in intensive care unit1 yearwhat treatments are used in intensive care unit to treat infection
Complications1 yearwhat are the complications due to severe infection
Treatments used in routine care unit1 yearwhich treatments are used in routine care unit to treat the infection
Risk factors1 yeardescription of underlying conditions
Characterization of Group A Streptococcus strains1 yearCharacterization of Group A Streptococcus strains by the CNR
Death1 yearDeath Outcome during hospitalisation

Countries

France

Contacts

Primary ContactLevy Corinne
corinne.levy@activ-france.fr1 48 85 04 04
Backup ContactBechet Stephane
stephane.bechet@activ-france.fr1 48 85 96 68

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026